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dc.contributor.authorParra-Izquierdo V
dc.contributor.authorFrías-Ordoñez J.S
dc.contributor.authorJuliao-Baños F
dc.contributor.authorCuadros C
dc.contributor.authorRomero Sanchez C
dc.contributor.authorFlórez-Sarmiento C.
dc.date.accessioned2024-10-09T14:28:39Z
dc.date.available2024-10-09T14:28:39Z
dc.date.issued2024
dc.identifier.issn2105705
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85175321207&doi=10.1016%2fj.gastrohep.2023.10.003&partnerID=40&md5=eba0eea6db05400f9c5b06696adcfc43
dc.identifier.urihttp://hdl.handle.net/10818/61978
dc.description.abstractIntroduction: Tofacitinib is indicated in patients with moderate to severe ulcerative colitis (UC); however, given its rapid onset of action, it may constitute an alternative in patients with hospitalized severe acute UC. There are few data on this indication in the literature. The aim of this study was to describe the efficacy and safety of tofacitinib in the management of patients with hospitalized UC, as well as its clinical characteristics and other treatment patterns. Materials and methods: Descriptive observational study of adults and children with CUAG treated with tofacitinib between June 2019 and December 2022 in Colombia. Sociodemographic and clinical variables were collected, therapeutic response was evaluated in different periods of time and descriptive analysis of quantitative and qualitative variables was performed. Results: Six patients (five adults and one pediatric), mean age 33.2 (SD: 8.5) years, with CUAG. Symptom remission was obtained in 100% of patients at day 7 after tofacitinib initiation. In three patients information was obtained beyond 6 months, with 100% clinical, biochemical, and endoscopic remission and without requiring colectomy. In the case of the pediatric patient, symptom remission was achieved one week after starting tofacitinib, remaining in clinical, biochemical and endoscopic remission beyond 6 months. No serious adverse events were reported in any of the cases. Conclusions: Tofacitinib represents a rescue therapeutic alternative in CUAG, with rapid clinical response, adequate tolerance and less need for colectomy, being sustained for periods beyond 6 months. © 2023 Elsevier España, S.L.U.en
dc.formatapplication/pdfes_CO
dc.language.isoenges_CO
dc.publisherGastroenterologia y Hepatologiaes_CO
dc.relation.ispartofseriesGastroenterologia y Hepatologia Vol. 47 N° 6
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceUniversidad de La Sabanaes_CO
dc.sourceIntellectum Repositorio Universidad de La Sabanaes_CO
dc.subject.otherDisease managementen
dc.subject.otherInflammatory bowel diseasesen
dc.subject.otherJanus kinase inhibitorsen
dc.subject.otherTherapeuticsen
dc.subject.otherTofacitiniben
dc.subject.otherUlcerative colitisen
dc.titleColombian experience with the use of tofacitinib in severe acute ulcerative colitis: A case series study [Experiencia colombiana con el uso de tofacitinib en colitis ulcerosa aguda grave: estudio de serie de casos]en
dc.typejournal articlees_CO
dc.type.hasVersionpublishedVersiones_CO
dc.rights.accessRightsopenAccesses_CO
dc.identifier.doi10.1016/j.gastrohep.2023.10.003


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